@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP170962.RA47HZ6IkdpYSKMbaTKooD4iU-yPysFG8CJUZeWxhgR4A> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP170962.RA47HZ6IkdpYSKMbaTKooD4iU-yPysFG8CJUZeWxhgR4A130_head {
  this: np:hasAssertion dgn-np:NP170962.RA47HZ6IkdpYSKMbaTKooD4iU-yPysFG8CJUZeWxhgR4A130_assertion ;
    np:hasProvenance dgn-np:NP170962.RA47HZ6IkdpYSKMbaTKooD4iU-yPysFG8CJUZeWxhgR4A130_provenance ;
    np:hasPublicationInfo dgn-np:NP170962.RA47HZ6IkdpYSKMbaTKooD4iU-yPysFG8CJUZeWxhgR4A130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP170962.RA47HZ6IkdpYSKMbaTKooD4iU-yPysFG8CJUZeWxhgR4A130_provenance a np:Provenance .
  dgn-np:NP170962.RA47HZ6IkdpYSKMbaTKooD4iU-yPysFG8CJUZeWxhgR4A130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP170962.RA47HZ6IkdpYSKMbaTKooD4iU-yPysFG8CJUZeWxhgR4A130_assertion {
  miriam-gene:1636 a ncit:C16612 .
  lld:C0027051 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP170962.RA47HZ6IkdpYSKMbaTKooD4iU-yPysFG8CJUZeWxhgR4A130_provenance {
  dgn-np:NP170962.RA47HZ6IkdpYSKMbaTKooD4iU-yPysFG8CJUZeWxhgR4A130_assertion dcterms:description "[ACE genotype distributions were not different between the Caucasian community control group and the CHD or the MI subgroups; the odds ratios and 95% confidence limits for the CHD group were 0.96 (0.73-1.27) for the D allele and 1.02 (0.80-1.31) for D homozygotes; for the MI group these values were 1.00 (0.83-1.20) and 0.99 (0.74-1.32) respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:11787479 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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}
dgn-np:NP170962.RA47HZ6IkdpYSKMbaTKooD4iU-yPysFG8CJUZeWxhgR4A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:32+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}